SCHEMBL1923328

SCHEMBL1923328

CCCCCCCCCOCc1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 4/20 0.58
TDP1 Q9NUW8 2/20 0.58
TSHR P16473 3/20 0.54
CETP P11597 3/20 0.51
LTA4H P09960 1/20 0.47
ALDH1A1 P00352 2/20 0.46
MAPK1 P28482 2/20 0.46
CYP3A4 P08684 1/20 0.46
DNM1 Q05193 1/20 0.46
APAF1 O14727 1/20 0.46
HRH4 Q9H3N8 1/20 0.45
HRH3 Q9Y5N1 1/20 0.45
HPGD P15428 1/20 0.45
MEN1 O00255 1/20 0.44
TP53 P04637 1/20 0.44
KMT2A Q03164 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
EPHX2 P34913 1/20 0.44

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL7517468 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL7120703 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL7641859 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL16057438 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL14526009 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL2886385 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL11995970 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL6685708 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL21081916 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL2231686 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 75 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3527593-B1 ISOCYANATE COMPOSITION, METHOD FOR PRODUCING ISOCYANATE COMPOSITION, AND METHOD FOR PRODUCING ISOCYANATE POLYMER ASAHI CHEMICAL IND (JP) 2025-07-23 EP disclosed
EP-3527600-B1 ISOCYANATE COMPOSITION AND PRODUCTION METHOD FOR ISOCYANATE POLYMER ASAHI CHEMICAL IND (JP) 2025-07-09 EP disclosed
CN-114456370-B Polyether anionic surfactant and method for improving oil and gas recovery ratio 中国石油化工股份有限公司 2024-01-26 CN disclosed
US-11826740-B2 Bridged phthalocyanine- and napththalocyanine-metal complex catalysts for oxidation reactions WISYS TECHNOLOGY FOUNDATION, INC. (US) 2023-11-28 US disclosed
CN-112979917-B Isocyanate composition, method for producing isocyanate composition, and method for producing isocyanate polymer 旭化成株式会社 2023-04-25 CN disclosed
US-20230114799-A1 ISOCYANATE COMPOSITION AND METHOD FOR PRODUCING ISOCYANATE POLYMER ASAHI KASEI KABUSHIKI KAISHA (JP) 2023-04-13 US disclosed
US-20230040510-A1 BRIDGED PHTHALOCYANINE- AND NAPTHTHALOCYANINE-METAL COMPLEX CATALYSTS FOR OXIDATION REACTIONS WISYS TECHNOLOGY FOUNDATION, INC. 2023-02-09 US disclosed
US-11548975-B2 Isocyanate composition and method for producing isocyanate polymer ASAHI KASEI KABUSHIKI KAISHA (JP) 2023-01-10 US disclosed
CN-109790269-B Isocyanate composition, method for producing isocyanate composition, and method for producing isocyanate polymer 旭化成株式会社 2022-06-14 CN disclosed
CN-109803992-B Isocyanate composition and method for producing isocyanate polymer 旭化成株式会社 2022-05-24 CN disclosed
US-20040138448-A1 Synthesis of non-symmetrical sulfamides using burgess-type reagents THE SCRIPPS RESEARCH INSTITUTE 2004-07-15 US disclosed
US-6719053-B2 A BASE FLUID AND A MONOESTER COPOLYMER OF STYRENE AND MALEIC ANHYDRIDE TO TREAT A SUBTERRANEAN FORMATION; HEAT RESISTANT AT TEMPERATURES OF >250 DEGRESS F.; PIPELINE TREATMENT, HYDRAULIC FRACTURING, WELL COMPLETION, GRAVEL PACKING, DRILLING FLUIDS BJ SERVICES COMPANY 2004-04-13 US disclosed
WO-2004007065-A1 METHOD FOR THE PRODUCTION OF EASILY POLYMERIZABLE COMPOUNDS BASF AKTIENGESELLSCHAFT (DE) 2004-01-22 WO disclosed
US-20030045605-A1 Ester/monoester copolymer compositions and methods of preparing and using same BJ SERVICES COMPANY 2003-03-06 US disclosed
CN-1175982-A Modifier for aldoxime extractant of metal useful component HENKEL CORP (US) 1998-03-11 CN disclosed
EP-0225602-B1 ALPHA-HYDROXYTHIO ETHERS CIBA-GEIGY AG (CH) 1991-10-09 EP disclosed
US-4808572-A ANTIALLERGENS CIBA-GEIGY CORPORATION (US) 1989-02-28 US disclosed
US-4745138-A ADHESION PONY INDUSTRIES, INC. (US) 1988-05-17 US disclosed
US-4722947-A ADHESION PROMOTERS OF BINDERS PONY INDUSTRIES, INC. (US) 1988-02-02 US disclosed
EP-0225602-A2 Alpha-hydroxythio ethers CIBA-GEIGY AG (CH) 1987-06-16 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11548975-B2 Isocyanate composition and method for producing isocyanate polymer IDH3A, IDH2, IDH3B L3MBTL1 4586/4885TDP1 3008/4885TSHR 4885/4885
US-20230040510-A1 BRIDGED PHTHALOCYANINE- AND NAPTHTHALOCYANINE-METAL COMPLEX CATALYSTS FOR OXIDATION REACTIONS NQO1, CYBB, PPOX L3MBTL1 4700/4885TDP1 3535/4885TSHR 4877/4885
US-20230114799-A1 ISOCYANATE COMPOSITION AND METHOD FOR PRODUCING ISOCYANATE POLYMER IDH3A, IDH2, IDH3B L3MBTL1 4577/4885TDP1 2789/4885TSHR 4885/4885
US-11826740-B2 Bridged phthalocyanine- and napththalocyanine-metal complex catalysts for oxidation reactions NQO1, CYBB, PPOX L3MBTL1 4700/4885TDP1 3535/4885TSHR 4877/4885
US-20040138448-A1 Synthesis of non-symmetrical sulfamides using burgess-type reagents SBDS, SRM, SMS L3MBTL1 3061/4885TDP1 3418/4885TSHR 1486/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.